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枳椇子乙醇提取物对耐甲氧西林金黄色葡萄球菌的抗菌活性研究及其抗菌机制的阐明。

Studies on antimicrobial activity of Poncirus trifoliata ethyl extract fraction against methicillin-resistant Staphylococcus aureus and to elucidate its antibacterial mechanism.

作者信息

Eom Sung-Hwan, Jung Yeoun-Joong, Lee Dae-Sung, Yim Mi-Jin, Kim Hye Seon, Lee Sang-Hoon, Myeong Jeong-In, Lee Jinhwan, Kim Hyun-Woo, Kim Kyoung-Ho, Lee Myung-Suk, Kim Young-Mog

出版信息

J Environ Biol. 2016 Jan;37(1):129-34.

PMID:26930870
Abstract

Traditional medicinal plants contain a wide variety of chemicals that have potent antibacterial activity. To find an alternative agent of overcoming the problems of methicillin-resistant Staphylococcus aureus (MRSA), the antibacterial mechanism of Ponciruss trifoliata against MRSA was investigated. Ethyl acetate (EtOAc)-soluble extract of P. trifoliata methanolic extract was evaluated for antibacterial activity using minimum inhibitory concentration (MIC). An EtOAc sub-fraction 08 (EA08) from silica-gel open column chromatography exhibited strong anti-MRSA activity. Apart from the study to isolate single compound from EA08, a synergistic antibacterial effect between the sub-fraction and β-lactam antibiotics against MRSA was determined. In order to elucidate the antibacterial restoring mechanism of EA08 on MRSA, mRNA expression of mecA gene and production penicillin-binding protein 2a (PBP2a) encoded by mecA gene were monitored. EA 08 showed the strongest antibacterial activity with MIC value of 256 μg ml(-1). MIC of oxacillin against MRSA was dramatically reduced from 512 to 16 μg ml(-1) in combination with 256 μg ml(-1) of EA08. The fractional inhibitory concentration index of oxacillin was measured at 0.53 in combination with EA08 against MRSA, suggesting that EA08-oxacillin combinations exert synergetic effect against MRSA. The analysis of RT-PCR and Western blotting profiles revealed that EA08 inhibited mRNA expression of mecA gene and production PBP2a, which is a key determinant for β-lactam antibiotic resistance, in a dose-dependent manner. These results indicated that EA08 eventually led to the reduction or inhibition of PBP2a production through translational inhibition in MRSA.

摘要

传统药用植物含有多种具有强大抗菌活性的化学物质。为了寻找一种克服耐甲氧西林金黄色葡萄球菌(MRSA)问题的替代药物,研究了枳椇对MRSA的抗菌机制。采用最低抑菌浓度(MIC)法评价了枳椇甲醇提取物的乙酸乙酯(EtOAc)可溶提取物的抗菌活性。硅胶开放柱色谱法得到的EtOAc亚组分08(EA08)表现出较强的抗MRSA活性。除了从EA08中分离单一化合物的研究外,还确定了该亚组分与β-内酰胺类抗生素对MRSA的协同抗菌作用。为了阐明EA08对MRSA的抗菌恢复机制,监测了mecA基因的mRNA表达以及由mecA基因编码的青霉素结合蛋白2a(PBP2a)的产生。EA 08表现出最强的抗菌活性,MIC值为256μg ml(-1)。与256μg ml(-1)的EA08联合使用时,苯唑西林对MRSA的MIC从512μg ml(-1)显著降低至16μg ml(-1)。苯唑西林与EA08联合对MRSA的部分抑菌浓度指数为0.53,表明EA08-苯唑西林联合对MRSA具有协同作用。RT-PCR和蛋白质印迹分析结果显示,EA08以剂量依赖的方式抑制mecA基因的mRNA表达和PBP2a的产生,PBP2a是β-内酰胺类抗生素耐药性的关键决定因素。这些结果表明,EA08最终通过对MRSA的翻译抑制导致PBP2a产生的减少或抑制。

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